proline has been researched along with Batten Turner Congenital Myopathy in 2 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 1 (50.00) | 18.2507 |
2000's | 1 (50.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Chang, LI; Chen, PR; Hsiao, KM; Jou, SB; Pan, H | 1 |
Dubowitz, V; Lehmann-Horn, F; Lerche, H; Mitrovic, N | 1 |
2 other study(ies) available for proline and Batten Turner Congenital Myopathy
Article | Year |
---|---|
Novel CLCN1 mutations in Taiwanese patients with myotonia congenita.
Topics: Adolescent; Adult; Aspartic Acid; Child; Chloride Channels; DNA Mutational Analysis; Female; Glycine; Humans; Isoleucine; Male; Mutation, Missense; Myotonia Congenita; Phenylalanine; Polymorphism, Genetic; Proline; Serine; Taiwan; Threonine | 2004 |
Paramyotonia congenita: the R1448P Na+ channel mutation in adult human skeletal muscle.
Topics: Adult; Arginine; Biopsy; Cold Temperature; Female; Hot Temperature; Humans; Ion Channel Gating; Isometric Contraction; Microelectrodes; Muscle Weakness; Muscle, Skeletal; Myotonia Congenita; Patch-Clamp Techniques; Point Mutation; Proline; Sodium Channels; Walking | 1996 |